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Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease
Calcium balance is abnormal in adults with chronic kidney disease (CKD) and is associated with the development of vascular calcification. It is currently not routine to screen for vascular calcification in CKD patients. In this cross-sectional study, we investigate whether the ratio of naturally occ...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989339/ https://www.ncbi.nlm.nih.gov/pubmed/36808527 http://dx.doi.org/10.1093/mtomcs/mfad009 |
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author | Dosseto, Anthony Lambert, Kelly Cheikh Hassan, Hicham I Fuller, Andrew Borst, Addison Dux, Florian Lonergan, Maureen Tacail, Theo |
author_facet | Dosseto, Anthony Lambert, Kelly Cheikh Hassan, Hicham I Fuller, Andrew Borst, Addison Dux, Florian Lonergan, Maureen Tacail, Theo |
author_sort | Dosseto, Anthony |
collection | PubMed |
description | Calcium balance is abnormal in adults with chronic kidney disease (CKD) and is associated with the development of vascular calcification. It is currently not routine to screen for vascular calcification in CKD patients. In this cross-sectional study, we investigate whether the ratio of naturally occurring calcium (Ca) isotopes, (44)Ca and (42)Ca, in serum could be used as a noninvasive marker of vascular calcification in CKD. We recruited 78 participants from a tertiary hospital renal center: 28 controls, 9 subjects with mild–moderate CKD, 22 undertaking dialysis and 19 who received a kidney transplant. For each participant, systolic blood pressure, ankle brachial index, pulse wave velocity, and estimated glomerular filtration rate were measured, along with serum markers. Calcium concentrations and isotope ratios were measured in urine and serum. While we found no significant association between urine Ca isotope composition (noted δ(44/42)Ca) between the different groups, δ(44/42)Ca values in serum were significantly different between healthy controls, subjects with mild–moderate CKD and those undertaking dialysis (P < 0.01). Receiver operative characteristic curve analysis shows that the diagnostic utility of serum δ(44/42)Ca for detecting medial artery calcification is very good (AUC = 0.818, sensitivity 81.8% and specificity 77.3%, P < 0.01), and performs better than existing biomarkers. Although our results will need to be verified in prospective studies across different institutions, serum δ(44/42)Ca has the potential to be used as an early screening test for vascular calcification. |
format | Online Article Text |
id | pubmed-9989339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99893392023-03-08 Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease Dosseto, Anthony Lambert, Kelly Cheikh Hassan, Hicham I Fuller, Andrew Borst, Addison Dux, Florian Lonergan, Maureen Tacail, Theo Metallomics Paper Calcium balance is abnormal in adults with chronic kidney disease (CKD) and is associated with the development of vascular calcification. It is currently not routine to screen for vascular calcification in CKD patients. In this cross-sectional study, we investigate whether the ratio of naturally occurring calcium (Ca) isotopes, (44)Ca and (42)Ca, in serum could be used as a noninvasive marker of vascular calcification in CKD. We recruited 78 participants from a tertiary hospital renal center: 28 controls, 9 subjects with mild–moderate CKD, 22 undertaking dialysis and 19 who received a kidney transplant. For each participant, systolic blood pressure, ankle brachial index, pulse wave velocity, and estimated glomerular filtration rate were measured, along with serum markers. Calcium concentrations and isotope ratios were measured in urine and serum. While we found no significant association between urine Ca isotope composition (noted δ(44/42)Ca) between the different groups, δ(44/42)Ca values in serum were significantly different between healthy controls, subjects with mild–moderate CKD and those undertaking dialysis (P < 0.01). Receiver operative characteristic curve analysis shows that the diagnostic utility of serum δ(44/42)Ca for detecting medial artery calcification is very good (AUC = 0.818, sensitivity 81.8% and specificity 77.3%, P < 0.01), and performs better than existing biomarkers. Although our results will need to be verified in prospective studies across different institutions, serum δ(44/42)Ca has the potential to be used as an early screening test for vascular calcification. Oxford University Press 2023-02-17 /pmc/articles/PMC9989339/ /pubmed/36808527 http://dx.doi.org/10.1093/mtomcs/mfad009 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Paper Dosseto, Anthony Lambert, Kelly Cheikh Hassan, Hicham I Fuller, Andrew Borst, Addison Dux, Florian Lonergan, Maureen Tacail, Theo Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
title | Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
title_full | Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
title_fullStr | Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
title_full_unstemmed | Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
title_short | Calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
title_sort | calcium isotopes as a biomarker for vascular calcification in chronic kidney disease |
topic | Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9989339/ https://www.ncbi.nlm.nih.gov/pubmed/36808527 http://dx.doi.org/10.1093/mtomcs/mfad009 |
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